北京大学学报(医学版) ›› 2009, Vol. 41 ›› Issue (4): 463-468.

• 疑难/罕见病例分析 • 上一篇    下一篇

肺玻璃样变肉芽肿病(英文稿)

Zhao-lin XU1△, Drew BETHUNE2, Daria MANOS3, Annette FOYLE1, Harry

  

  1. HENTELEFF2,Michael JOHNSTON2 , Yannick CARTIER3(1.Departments of Pathology, 2. Departments of Surgery, 3. Departments of Radiology, Queen Elizabeth Ⅱ Health Sciences Centre and Dalhousie University, Halifax, Nova Sciotia, Canada B3H 1V8)
  • 收稿日期:2009-06-22 修回日期:1900-01-01 出版日期:2009-08-18 发布日期:2009-08-18
  • 通讯作者: xuzhaolin

  • Received:2009-06-22 Revised:1900-01-01 Online:2009-08-18 Published:2009-08-18

摘要:

关键词: 肉芽肿, 浆细胞, 肺, 肺肿瘤, 病理学, 肺炎

Abstract: Objective: To present clinical and pathologic features of pulmonary hyalnizing granuloma through analyzing three cases found in our institution and reviewing cases reported in the English language literature.Methods and Results: Three cases of pulmonary hyalnizing granuloma identified at our institution during the past ten years were reviewed. In the first case, the patient presented with concurrent pulmonary hyalinizing granuloma and histoplasmosis. In the second case, the patient presented with a 5.5 cm lung mass and a separate smaller lesion radiologically resembling bronchogenic carcinoma. There was very prominent polyclonal lymphocytic proliferation at the periphery especially of the smaller lesion likely representing an early stage of the disease process. In the third case, the patient presented with multiple subpleural plaque-like lesions in addition to nodular lesions of the lung. All cases also demonstrated various degrees of lymphocytic infiltration within the lesions. The English literature has been reviewed through searching the PubMed.Conclusion: Since patients with pulmonary hyalinizing granuloma demonstrated a spectrum of clinical presentations, radiologic changes and histologic features with a variety of associated clinical disorders, pulmonary hyalnizing granuloma is more in keeping with a clinicopathologic entity rather than a specific pathologic disease.

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